Canonical Allele Identifier: CA1398327465
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123284662C= , CM000665.2:g.123284662C= GRCh38
NC_000003.11:g.123003509C= , CM000665.1:g.123003509C= GRCh37
NC_000003.10:g.124486199C= NCBI36
NG_033882.1:g.168884G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.2409G= ENSP00000420082.2:p.Lys803=
ENST00000470367.2:c.2697G= ENSP00000514541.1:p.Lys899=
ENST00000483566.2:c.2409G= ENSP00000420252.2:p.Lys803=
ENST00000699714.1:c.2409G= ENSP00000514539.1:p.Lys803=
ENST00000699715.1:c.2409G= ENSP00000514540.1:p.Lys803=
ENST00000699716.1:c.2409G= ENSP00000514542.1:p.Lys803=
ENST00000699717.1:n.2135G=
ENST00000699718.1:c.3807G= ENSP00000514543.1:p.Lys1269=
ENST00000462833.6:c.3732G= MANE Select ENSP00000419361.1:p.Lys1244=
ENST00000309879.9:c.2682G= ENSP00000308685.5:p.Lys894=
ENST00000462833.5:c.3732G= ENSP00000419361.1:p.Lys1244=
ENST00000478092.1:n.502G=
ENST00000491190.5:c.2706G= ENSP00000418537.1:p.Lys902=
NM_001199642.1:c.2682G= NP_001186571.1:p.Lys894=
NM_183357.2:c.3732G= NP_899200.1:p.Lys1244=
XM_005247077.2:c.3807G= XP_005247134.1:p.Lys1269=
XM_005247078.1:c.2757G= XP_005247135.1:p.Lys919=
XM_006713483.1:c.2706G= XP_006713546.1:p.Lys902=
XM_006713484.1:c.2484G= XP_006713547.1:p.Lys828=
XM_011512359.1:c.2808G= XP_011510661.1:p.Lys936=
XM_011512360.1:c.2718G= XP_011510662.1:p.Lys906=
XM_011512361.1:c.2484G= XP_011510663.1:p.Lys828=
XM_005247077.4:c.3807G= XP_005247134.1:p.Lys1269=
XM_011512359.2:c.2808G= XP_011510661.1:p.Lys936=
XM_011512360.3:c.2718G= XP_011510662.1:p.Lys906=
XM_017005638.1:c.2709G= XP_016861127.1:p.Lys903=
XM_017005639.1:c.2709G= XP_016861128.1:p.Lys903=
NM_001378259.1:c.3807G= NP_001365188.1:p.Lys1269=
NM_183357.3:c.3732G= MANE Select NP_899200.1:p.Lys1244=